Product Recalls in New Jersey
Product recalls affecting New Jersey — including food, drugs, consumer products, medical devices, and vehicles distributed to New Jersey. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,060 recalls have been distributed to New Jersey in the last 12 months.
Showing 24941–24960 of 53,621 recalls
Recalled Item: Smith&Nephew SmartStitch PerfectPasser Connector Recalled by ArthroCare...
The Issue: The voluntary recall is being initiated due to a manufacturing error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Macleods...
The Issue: CGMP Deviation: Presence of NDEA (N-Nitrosodimethylamine), a carcinogen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxybutynin Chloride Recalled by Lannett Company Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS¿ ECi/ECiQ Immunodiagnostic System Product Code: 1922814 For use in...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELL-DYN Emerald analyzer Recalled by Abbott Laboratories Due to There is a...
The Issue: There is a potential for the device to generate Quality Control (QC) low or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 3600 Immunoassay System-Software V3.3.2 & below Product Code:...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 3600 Immunoassay System V3.3.2 & below Product Code: Recalled by...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES Extraction Kit Recalled by Luminex Corporation Due to Through internal...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aries Bordetella Assay Recalled by Luminex Corporation Due to Through...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES Group A Strep Assay Recalled by Luminex Corporation Due to Through...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES GBS Assay Recalled by Luminex Corporation Due to Through internal...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES Flu A/B & RSV Assay Recalled by Luminex Corporation Due to Through...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES C. difficile Assay Recalled by Luminex Corporation Due to Through...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ XT 7600 Integrated System-Software V3.4.1 & below Product Code:...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS ECi Immunodiagnostic System Product Code: 6801059 For use Recalled by...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 5600 Integrated System V3.3.2 & below Product Code: Recalled by...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 5600 Integrated System -Software V3.3.2 & below Product Code:...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES HSV 1&2 Assay Recalled by Luminex Corporation Due to Through internal...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Victoria Marinara Sauce Recalled by B&G Foods North America, Inc Due to...
The Issue: Product may contain undeclared cashews.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Meijer Ultimate Chocolate Mint Chip Cookie Cookies in clear plastic Recalled...
The Issue: Undeclared soy
Recommended Action: Do not consume. Return to store for a refund or discard.